Evidence map›Paper›PMID 36575058›Full record

ArticleEuropean heart journal. Cardiovascular Imaging2023

Emerging molecular imaging targets and tools for myocardial fibrosis detection.

Anna K Barton, Evangelos Tzolos, Rong Bing, Trisha Singh, Wolfgang Weber, Markus Schwaiger, Zohreh Varasteh, Riemer H J A Slart, David E Newby, Marc R Dweck

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in European heart journal. Cardiovascular Imaging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07583173 (A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Effect of Finerenone on Myocardial Fibrosis and Cardiac Structure and Function in Heart Failure Patients With Mildly Reduced or Preserved Ejection Fraction), which is not on this map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
7.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07583173 phase4not yet recruitingnot on this mapstarted 2026, after this paper: background citation

A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Effect of Finerenone on Myocardial Fibrosis and Cardiac Structure and Function in Heart Failure Patients With Mildly Reduced or Preserved Ejection Fraction

TypeinterventionalSponsorChina National Center for Cardiovascular DiseasesRan2026 to 2027Enrolled104ConditionsHeart FailureArmsOral finerenone, Placebo
3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Translational biology of human cardiac fibrosis.Nature cardiovascular research · 2026
    Review
  3. Article
  4. Next-generation molecular imaging of cardiac fibrosis.The international journal of cardiovascular imaging · 2026
    Review
  5. European journal of nuclear medicine and molecular imaging · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Observational
  16. SNMMI Procedure Standard/EANM Practice Guideline for Fibroblast Activation Protein (FAP) PET.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2025
    Article
  17. Article
  18. Prognostic value ofFrontiers in cardiovascular medicine · 2025
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Anna K BartonBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, Little France Crescent, Edinburgh EH16 4SB, UK.ORCID 0000-0002-7953-3015
Evangelos TzolosBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, Little France Crescent, Edinburgh EH16 4SB, UK.ORCID 0000-0003-0038-043X
Rong BingBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, Little France Crescent, Edinburgh EH16 4SB, UK.ORCID 0000-0002-8305-4906
Trisha SinghBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, Little France Crescent, Edinburgh EH16 4SB, UK.
Wolfgang WeberDepartment of Nuclear Medicine, Clinikum rechts der Isar, Technical University of Munich, Ismaniger Straße 22, 81675 Munich, Germany.
Markus SchwaigerDepartment of Nuclear Medicine, Clinikum rechts der Isar, Technical University of Munich, Ismaniger Straße 22, 81675 Munich, Germany.
Zohreh VarastehDepartment of Nuclear Medicine, Clinikum rechts der Isar, Technical University of Munich, Ismaniger Straße 22, 81675 Munich, Germany.
Riemer H J A SlartFaculty of Medical Sciences, University of Groningen, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands.
David E NewbyBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, Little France Crescent, Edinburgh EH16 4SB, UK.
Marc R DweckBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Chancellor's Building, Little France Crescent, Edinburgh EH16 4SB, UK.ORCID 0000-0001-9847-5917
British Heart Foundation · GBTUM Klinikum · DEUniversity of Groningen · NL

Funding

British Heart Foundation CH/09/002/26360British Heart Foundation PG/19/40/34422British Heart Foundation RG/16/10/32375British Heart Foundation SS/CH/09/002/26360Medical Research Council G0701127Medical Research Council MR/T029153/1Medical Research Council T029153
6 · The paper itself

Abstract

Myocardial fibrosis is the heart's common healing response to injury. While initially seeking to optimize the strength of diseased tissue, fibrosis can become maladaptive, producing stiff poorly functioning and pro-arrhythmic myocardium. Different patterns of fibrosis are associated with different myocardial disease states, but the presence and quantity of fibrosis largely confer adverse prognosis. Current imaging techniques can assess the extent and pattern of myocardial scarring, but lack specificity and detect the presence of established fibrosis when the window to modify this process may have ended. For the first time, novel molecular imaging methods, including gallium-68 (68Ga)-fibroblast activation protein inhibitor positron emission tomography (68Ga-FAPI PET), may permit highly specific imaging of fibrosis activity. These approaches may facilitate earlier fibrosis detection, differentiation of active vs. end-stage disease, and assessment of both disease progression and treatment-response thereby improving patient care and clinical outcomes.

Indexed as

CardiomyopathiesFibrosisHumansMolecular ImagingMyocardiumPositron-Emission TomographyPositron Emission Tomography Computed Tomographyfibroblast activation protein inhibitorfibrosis imagingmolecular fibrosis imagingmyocardial fibrosispositron emission tomography and cardiovascular magnetic resonance

Identifiers

PMID36575058
PMCPMC9936837
OpenAlexW4313236551

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.